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About the role ICON and you Application Process Day in the life Who we are

Clinical Data Analyst

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About the role

This vacancy has now expired. Please click here to view live vacancies.
Are you passionate about improving the quality of human life?    If so, we invite you to learn more about our home-based CLINICAL DATA ANALYST opportunity......
 
 ICON Clinical Research has a strong reputation in our approaches to clinical development.   We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients.   We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain. 
We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally.  We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients. 
 
CLINICAL DATA ANALYST
 
HOME BASED - ANY GLOBAL LOCATION
 
ROLE OVERVIEW
• Responsible for reviewing data based on the Triggers identified for one or more studies under the direction of the Central Monitoring Team Manager (CMTM) supervision.
• More specifically:
- Review study data accurately using Spotfire and other tools to identify site performance
- Raise findings (indicators of site performance issues) within the findings module of ICOTrial,
- Communicate effectively with the project team, CTM, CRAs, OM Staff, Medical staff, Scientific Council to ensure effective resolution of site performance issues.
- Ensure all timelines for CDA activities are completed within the required study timelines.
- Work with Data Management, Clinical Operations, Central Laboratory, lTG, Biostatistics, Medical Writing, Regulatory Affairs and Quality Assurance to ensure all data collected within a clinical study are managed according to corporate standards and meet regulatory guidelines for data integrity.
 
To secure this exciting role, you will need:
  • Bachelor's degree or local equivalent in a scientific discipline and/or appropriate experience
  • The ideal candidate will have at least 3-4 years clinical data management or clinical research associate (CRA) experience.
  • Knowledge of regulatory requirements respecting data quality and clinical trials conduct
  • Excellent oral communication skills.
  • Excellent accuracy and attentiveness to detail.
  • Proven leadership skills and the ability to work independently to resolve study related issues
  • Ability to work within a team environment with excellent interpersonal skills
  • Ability to manage competing priorities in a changeable environment and the ability to handle stressful situations and deadlines;
  • Knowledge of database technologies and processes.
 BENEFITS 
We support our employees to achieve a good work/home life balance and offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an incentive plan for strong performers. Additionally, we have cutting edge technology to ensure better outcomes. 
 
 We invite you to review all our opportunities at www.iconplc.com/careers.
 
 ICON is an equal opportunity employer -  M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 
Closing date: Friday 11.04.2014
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